Yong Qian, Yuxiao Lin, Jinwei Tian, Wei Xia, Xianya Li, Ning Lin
{"title":"预建气体纳米室战略:为钠离子电池生产富含封闭孔隙和 sp2-C 的硬碳","authors":"Yong Qian, Yuxiao Lin, Jinwei Tian, Wei Xia, Xianya Li, Ning Lin","doi":"10.1016/j.ensm.2025.104092","DOIUrl":null,"url":null,"abstract":"Hard carbon still faces the challenge of incompatibility between high capacity and high initial Coulombic efficiency (ICE). Herein, a pre-construction gas nanochamber strategy is proposed to produce hard carbon with abundant closed pores and sp<sup>2</sup>-C, thereby simultaneously achieving high capacity and ICE. The gas nanochambers are engineered by balancing the self-generated pressure and external pressure during the carbon precursor pyrolysis. A combination of in-situ/ex-situ characterizations and molecular dynamics (MD) simulations reveal that the external pressure can restrict the intense release the pyrolyzed gases, thus forming abundant and uniform nanochamber-like close pores within macroparticles. Concurrently, the intervention of pressure facilitates the arrangement of carbon atoms into sp<sup>2</sup>-C with a few defects. Further insights from bulk phase/interface analysis and density functional theory (DFT) calculations demonstrate that this unique structure enables hard carbon to store more sodium ions and preferentially decompose NaPF<sub>6</sub> to form an inner inorganic-rich solid electrolyte interface (SEI) film. As a result, the optimized hard carbon can deliver high capacity of 370.4 mA h g<sup>−1</sup> with ICE of 89.3%, excellent rate capability and long-term cycling stability with a capacity of 136.1 mA h g<sup>−1</sup> after 10000 cycles at 5.0 A g<sup>−1</sup>.","PeriodicalId":306,"journal":{"name":"Energy Storage Materials","volume":"40 1","pages":""},"PeriodicalIF":18.9000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pre-construction Gas Nanochamber Strategy: Producing Hard Carbon Rich in Closed Pores and sp2-C for Sodium-ion Batteries\",\"authors\":\"Yong Qian, Yuxiao Lin, Jinwei Tian, Wei Xia, Xianya Li, Ning Lin\",\"doi\":\"10.1016/j.ensm.2025.104092\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hard carbon still faces the challenge of incompatibility between high capacity and high initial Coulombic efficiency (ICE). Herein, a pre-construction gas nanochamber strategy is proposed to produce hard carbon with abundant closed pores and sp<sup>2</sup>-C, thereby simultaneously achieving high capacity and ICE. The gas nanochambers are engineered by balancing the self-generated pressure and external pressure during the carbon precursor pyrolysis. A combination of in-situ/ex-situ characterizations and molecular dynamics (MD) simulations reveal that the external pressure can restrict the intense release the pyrolyzed gases, thus forming abundant and uniform nanochamber-like close pores within macroparticles. Concurrently, the intervention of pressure facilitates the arrangement of carbon atoms into sp<sup>2</sup>-C with a few defects. Further insights from bulk phase/interface analysis and density functional theory (DFT) calculations demonstrate that this unique structure enables hard carbon to store more sodium ions and preferentially decompose NaPF<sub>6</sub> to form an inner inorganic-rich solid electrolyte interface (SEI) film. As a result, the optimized hard carbon can deliver high capacity of 370.4 mA h g<sup>−1</sup> with ICE of 89.3%, excellent rate capability and long-term cycling stability with a capacity of 136.1 mA h g<sup>−1</sup> after 10000 cycles at 5.0 A g<sup>−1</sup>.\",\"PeriodicalId\":306,\"journal\":{\"name\":\"Energy Storage Materials\",\"volume\":\"40 1\",\"pages\":\"\"},\"PeriodicalIF\":18.9000,\"publicationDate\":\"2025-02-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy Storage Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ensm.2025.104092\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Storage Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.ensm.2025.104092","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Pre-construction Gas Nanochamber Strategy: Producing Hard Carbon Rich in Closed Pores and sp2-C for Sodium-ion Batteries
Hard carbon still faces the challenge of incompatibility between high capacity and high initial Coulombic efficiency (ICE). Herein, a pre-construction gas nanochamber strategy is proposed to produce hard carbon with abundant closed pores and sp2-C, thereby simultaneously achieving high capacity and ICE. The gas nanochambers are engineered by balancing the self-generated pressure and external pressure during the carbon precursor pyrolysis. A combination of in-situ/ex-situ characterizations and molecular dynamics (MD) simulations reveal that the external pressure can restrict the intense release the pyrolyzed gases, thus forming abundant and uniform nanochamber-like close pores within macroparticles. Concurrently, the intervention of pressure facilitates the arrangement of carbon atoms into sp2-C with a few defects. Further insights from bulk phase/interface analysis and density functional theory (DFT) calculations demonstrate that this unique structure enables hard carbon to store more sodium ions and preferentially decompose NaPF6 to form an inner inorganic-rich solid electrolyte interface (SEI) film. As a result, the optimized hard carbon can deliver high capacity of 370.4 mA h g−1 with ICE of 89.3%, excellent rate capability and long-term cycling stability with a capacity of 136.1 mA h g−1 after 10000 cycles at 5.0 A g−1.
期刊介绍:
Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field.
Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy.
Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.